BEUDAMED
    4 results · 20ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    Rampart D Lumbar Interbody Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INTERLINK SYSTEM-T-CONNECTOR EXTENSION SET, MODEL 2N3326

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

    Set, Administration, Intravascular

    FDA classification
    FDA Class 2 ·Set, Administration, Intravascular